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Physical Review A

Spontaneous emission of an excited atom in a random absorbing medium (6 pages)

Wei Guo

Published Jan 1, 2004• 0 citations
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The decay rate of an excited molecule (atom) embedded in a dispersive and absorbing planar cavity is derived by using a recently obtained compact form of the Green's function for a multilayer. As a by-product, a hint is provided for a straightforward extension of the results obtained for lossless cavities of other shapes to the corresponding absorbing cavities. The decay rate in an absorbing cavity consists of the spontaneous emission rate and of the nonradiative rates caused by the near-field interaction of the molecule with the cavity medium and, for nearby molecules, with the cavity mirrors. Only the spontaneous emission rate is satisfactorily described in the macroscopic approach adopted. The theory is applied to an analysis of the effects of the weak cavity absorption on the decay rate in a dielectric microcavity formed by two metallic mirrors. As expected, dissipation in the cavity medium spoils the conditions for controlled spontaneuos emission and strongly suppresses the intensity of spontaneous emission. However, its effect on the spontaneous emission rate is much less pronounced.

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Spontaneous emission and level shifts in absorbing disordered dielectrics and dense atomic gases: A Green’s-function approach

Michael Fleischhauer

Spontaneous emission and Lamb shift of atoms in absorbing dielectrics and dense atomic gases are discussed using a microscopic Green's-function approach. Uncorrelated and random atomic positions are assumed, and the associated unphysical interactions between different atoms at the same location are eliminated (local field correction). For the case of an atom in a purely dispersive medium, the spontaneous-emission rate is altered by the well-known Lorentz local-field factor. When the mean distance between atoms becomes less than the resonance wavelength, results different from previously suggested expressions are found. In particular, it is shown that nearest-neighbor interactions become important. The results suggest that, for large densities, absorbing disordered dielectrics cannot accurately be described by a macroscopic approach that neglects correlations between atomic positions.

arXiv:quant-ph/9902076•Physical Review A•Sep 1, 1999•44 citations
The decay rate of an excited molecule (atom) embedded in a dispersive and absorbing planar cavity is derived by using a recently obtained compact form of the Green's function for a multilayer. As a by-product, a hint is provided for a straightforward extension of the results obtained for lossless cavities of other shapes to the corresponding absorbing cavities. The decay rate in an absorbing cavity consists of the spontaneous emission rate and of the nonradiative rates caused by the near-field interaction of the molecule with the cavity medium and, for nearby molecules, with the cavity mirrors. Only the spontaneous emission rate is satisfactorily described in the macroscopic approach adopted. The theory is applied to an analysis of the effects of the weak cavity absorption on the decay rate in a dielectric microcavity formed by two metallic mirrors. As expected, dissipation in the cavity medium spoils the conditions for controlled spontaneuos emission and strongly suppresses the intensity of spontaneous emission. However, its effect on the spontaneous emission rate is much less pronounced.
Spontaneous emission and Lamb shift of atoms in absorbing dielectrics and dense atomic gases are discussed using a microscopic Green's-function approach. Uncorrelated and random atomic positions are assumed, and the associated unphysical interactions between different atoms at the same location are eliminated (local field correction). For the case of an atom in a purely dispersive medium, the spontaneous-emission rate is altered by the well-known Lorentz local-field factor. When the mean distance between atoms becomes less than the resonance wavelength, results different from previously suggested expressions are found. In particular, it is shown that nearest-neighbor interactions become important. The results suggest that, for large densities, absorbing disordered dielectrics cannot accurately be described by a macroscopic approach that neglects correlations between atomic positions.